CN1895048B - Synergistic insecticidal mixtures - Google Patents

Synergistic insecticidal mixtures Download PDF

Info

Publication number
CN1895048B
CN1895048B CN2006101001990A CN200610100199A CN1895048B CN 1895048 B CN1895048 B CN 1895048B CN 2006101001990 A CN2006101001990 A CN 2006101001990A CN 200610100199 A CN200610100199 A CN 200610100199A CN 1895048 B CN1895048 B CN 1895048B
Authority
CN
China
Prior art keywords
reactive compound
activity
solvent
emulsifier
methyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CN2006101001990A
Other languages
Chinese (zh)
Other versions
CN1895048A (en
Inventor
W·安德施
C·埃尔德伦
P·耶施克
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer Intellectual Property GmbH
Original Assignee
Bayer CropScience AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=7713432&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CN1895048(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Publication of CN1895048A publication Critical patent/CN1895048A/en
Application granted granted Critical
Publication of CN1895048B publication Critical patent/CN1895048B/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/24Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
    • A01N43/26Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
    • A01N43/28Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N51/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N53/00Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The invention relates to insecticidal mixtures containing a compound of formula (I) and at least one other known agent from the series abamectin, emamectin or emamectin benzoate, methiocarb, ss-cyfluthrin, and lambda-cyhalothrin. Also disclosed is the use of said mixtures for protecting plants from infestations by parasites.

Description

Synergistic insecticidal mixtures
The application is dividing an application of application number is 03807691.8, the applying date is on January 20th, 2003 patent application.
Technical field
The present invention relates to new reactive compound combination, wherein at first comprise known reactive compound Clothianidin and next at least a other known insecticidal active compound, said combination has very good desinsection and acaricide properties.
Background technology
Clothianidin shown in the known following formula
Figure S061A0199020060720D000011
Can be used for preventing and treating animal pest, particularly insect (referring to EP-A-376279 and EP 375907).This compound has excellent activity; Yet, under low rate of application or for anti-indivedual insects, it is unsatisfactory sometimes.
Also known compound Olivomitecidin (II) (DE 2717040), Emamectin (III) or Emamectin benzoate (IIIa) (EP 089202), mercaptodimethur (IV) (US3; 313,684), β-cyfloxylate (V) (EP 206149) and λ-cyhalothrin (VI) (EP106469) can be used for preventing and treating insect and/or mite class.
Summary of the invention
Have been found that now and comprise Clothianidin shown in the formula (I)
Figure S061A0199020060720D000012
Have synergistic activity with at least a compound (II), (III), (IIIa), (IV), (V) and mixture (VI), and be suitable for preventing and treating animal pest.Because this synergy can be used the much little reactive compound of its amount, promptly the activity of this mixture is greater than the activity of single component.
The ratio of used formula (I) compound and formula (II)-(VI) compound and total consumption of this mixture depend on the kind and the generation of insect and/or mite class.Use for each, can confirm the optimal proportion and total consumption that under each concrete condition, use through campaign.
Preferred mixture of the present invention comprises Clothianidin shown in the reactive compound formula (I) and Olivomitecidin (II).Olivomitecidin is also referring to " The Pesticide Manual ", 11 ThEdition, British Crop Protection Council, 1997, p3.
In this mixture, the ratio of reactive compound can change in relative broad range.The weight ratio of Clothianidin and Olivomitecidin is preferably 1: 1-50: 1, particularly 5: 1-25: 1.
Another preferred mixture of the present invention comprises Clothianidin shown in the reactive compound formula (I) and Emamectin (III) or Emamectin benzoate (IIIa).Emamectin and Emamectin salt is at Journal of Organic Chemistry, Vol.59 (1994), 7704-7708, US-P-4,4874,794, US-P-5,5,288,710 with EP-00089202 in also be called MK-244.
In this mixture, the ratio of reactive compound can change in relative broad range.The weight ratio of Clothianidin and Emamectin or Emamectin benzoate is preferably 1: 1-500: 1, particularly 100: 1-500: 1.
Another preferred mixture of the present invention comprises Clothianidin shown in the reactive compound formula (I) and mercaptodimethur (IV).Mercaptodimethur (IV) is also referring to " The PesticideManual ", 11 ThEdition, British Crop Protection Council, 1997, p 813.
In this mixture, the ratio of reactive compound can change in relative broad range.The weight ratio of Clothianidin and mercaptodimethur is preferably 1: 1-1: 10, particularly 1: 1-1: 5.
Another preferred mixture of the present invention comprises Clothianidin shown in the reactive compound formula (I) and β-cyfloxylate (V).β-cyfloxylate is also referring to " ThePesticide Manual ", 11 ThEdition, British Crop ProtectionCouncil, 1997, p 295.
In this mixture, the ratio of reactive compound can change in relative broad range.The weight ratio of Clothianidin and β-cyfloxylate is preferably 1: 1-10: 1, particularly 1: 1-6: 1.
Another preferred mixture of the present invention comprises Clothianidin shown in the reactive compound formula (I) and λ-cyhalothrin (VI).λ-cyhalothrin (VI) is also referring to " ThePesticide Manual ", 11 ThEdition, British Crop ProtectionCouncil, 1997, p 300.
In this mixture, the ratio of reactive compound can change in relative broad range.The weight ratio of Clothianidin and λ-cyhalothrin is preferably 1: 1-10: 1, be preferably 1: 1-6: 1.
Reactive compound combination of the present invention is suitable for controlling animal pest; Particularly in the protection of agricultural, forestry, storage product and material; And the insect of taking place in the health field, mite class and nematode, have good plant tolerance simultaneously and to the acceptable toxicity of warm blooded animal.They can be preferably used as the crop protection agent.They all have activity to normal sensitivity and resistance kind and to all or some developmental stage.Above-mentioned insect comprises:
Isopoda, for example, damp worm (Oniscus asellus), armadillidum vulgare, pillworm.
Doubly sufficient order, for example, tool zebra land.
Lip foot order, for example, food fruit DIWUGONG, common house centipede belong to.
Comprehensive order, for example, the flower garden common house centipede.
Thysanoptera, for example, the Taiwan silverfish.
Collembola, for example, the arms Onychiurus arcticus.
Orthoptera, for example, acheta domestica, Gryllotalpa spp, African migratory locust, black locust belong to and desert locust.
Blattaria, for example, oriental cockroach, American cockroach, Ma Dela blattaria and Groton bug.
Dermaptera, for example, European earwig.
Isoptera, for example, Reticulitermes.
Anoplura, for example, body louse, Haematopinus, jaw lice genus, Trichodectes and Damalinia.
Thrips, for example, greenhouse Hercinothrips spp, onion thrips, palm thrips and alfalfa thrips.
Heteroptera, for example, Eurygasterspp genus, red cotton bug (Dysdercus intermedius), square butt stinkbug, bed bug, phodnius prolixus and vertebra Reduvius.
Homoptera; For example, wild cabbage aleyrodid, sweet potato whitefly, Trialeurodes vaporariorum Westwood, cotten aphid, cabbage aphid, the latent knurl aphid of tea, beans winged euonymus aphid, apple aphid, wooly aphis, mealy plum aphid, grape phylloxera, goitre woolly aphid genus, English grain aphid, tumor aphid genus, phorodon aphid, rhopalosiphum padi, green jassids belong to, bring disaster to leafhopper (Euscelis bilobatus), rice leafhopper, the hard ball a red-spotted lizard of Europe fruit, olive pearl lecanium, small brown rice planthopper, brown planthopper, red kidney Aspidiotus, ivy Aspidiotus, mealybug genus and Psylla spp.
Lepidoptera; For example, pink bollworm, loose powder butterfly geometrid moth, orchard autumn geometrid moth, the thin moth of leaf mining (lithocolletis blancardella), apple ermine moth, diamond-back moth, malacosoma neustria, pornography and drug moth, Euproctis, cotton lyonetid (Bucculatrix thutberiella), phyllocnistis citrella stainton, Noctua, cut Noctua, dirty noctuid, Egyptian noctuid, Heliothis, tomato moth, small noctuid, Spodoptera, cabbage looper, codling moth, Pier, straw borer spp, corn borer, Anagasta kuehniella, galleria mellonella waxmoth, curtain rain moth, bag rain moth, brown moth, yellow tail leaf roller, cigarette moth (Capua reticulana), dragon spruce Choristoneura spp, grape codling moth (Clysia ambiguella), tea long paper moth, the green volume of oak moth, Cnaphalocerus genus and the Oulema oryzae knitted of boring cut.
Coleoptera; For example, furniture death watch beetle, lesser grain borer, bean weevil (Bruchidius obtectus), acanthoscelides obtectus, North America house longhorn beetle, blue hair stern firefly are chrysomelid, colorado potato beetles, horseradish ape are chrysomelid, the chrysomelid genus of bar, rape golden head flea beetle, mexican bean ladybird, latent food first genus, saw-toothed grain beetle, flower resemble genus, Sitophilus, vine black ear beak resemble, the banana collar resembles, seed resembles, alfalfa leaf resembles, khapra beetle belongs to, spot khapra beetle genus, Anthrenus, fur moth-eatenly belong to, the moth-eaten genus of powder, pollen beetle, Ptinus, golden spider beetle, wheat ptinid, Tribolium, bloom first, click beetle belong to, wide chest click beetle genus, May gill cockchafer, potato gill cockchafer, the brown New Zealand rib wing melolonthid and rice water resemble.
Hymenoptera, for example, pine sawfoy genus, real tenthredinidae, hair ant genus, MonomoriumMayr and Vespa.
Diptera; For example, Aedes, Anopheles, Culex, drosophila yellow gorilla, Musca, Fannia, calliphora erythrocephala, Lucilia, Carysomyia, cuterbrid genus, Gasterophilus, Hippobosca, Genus Stomoxys, Oestrus, Hypoderma, Gadfly, a smaller kind of cicada cicada belong to (Tannia spp.), garden march fly, Sweden's wheat stem chloropid fly, careless Hylemyia, spinach spring fly, Mediterranean fruitfly, olive fruit fly, marsh daddy-longlegs, Hylemyia and liriomyza bryoniae and belong to.
Siphonaptera, for example, Xanthopsyllacheopis and Ceratophyllus.
Arachnids; For example, scorpion (Scorpio maurus), erythema spider, Acarus siro, Argas, Ornithodorus, Dermanyssus gallinae, rabbit goitre mite, oranges and tangerines wrinkle leaf Aculus, Boophilus, Rh, Amblyomma, Hyalomma, hard tick genus, scabies mite genus, Psoroptes, itch mite genus, tarsonemid genus, Bryobia praetiosa, Panonychus citri genus, Tetranychus, half tarsonemid belong to and short whisker Acarapis.
Plant nematode comprises, for example Pratylenchidae genus, similar similes thorne, fuller's teasel stem eelworm, partly puncture that nematode, different skin belong to, the different skin of ball belongs to, root knot genus, Aphelenchoides, minute hand Turbatrix, sword line belong to, burr belongs to and the umbrella Aphelenchoides.
According to the present invention, can handle all plants and plant part.Plant is appreciated that and is all plants and plant community such as needs and unwanted wild plant or crops (comprising the crops that nature grows) here.Crops can be the plants that obtains through conventional plant breeding and optimization method or the combination through biotechnology and gene engineering method or said method, comprise genetically modified plants and comprise and can obtain maybe can not obtain the plant variety that the plant variety method is protected.The part of plant is interpreted as all ground and under ground portion and organs of plant, and like stem, leaf, Hua Hegen, the instance that can mention is blade, needle, petiole, trunk, flower, fruit body, fruit, seed, root, stem tuber and root-like stock.The plant each several part also comprises the plant and the asexual and sexual propagation material of results, for example cutting, stem tuber, root-like stock, layer and seed.
Adopting the processing method of the present invention of reactive compound combination carrying out plant and plant part is directly to use or compound effects is handled in their environment, habitat or storage area through conventional treatment method, for example floods, sprays, fumigates, atomizing, broadcasts sowing, brushes and particularly can also carry out one or more layers dressing under the situation of seed at propagating materials.
Reactive compound of the present invention combination can be converted to into conventional formulation such as solution, emulsion, wetting powder, suspending agent, pulvis, pulvis subtilis, paste, soluble powder, granule, dense suspended emulsion, with the microcapsule formulations of natural and the synthetic material and the polymeric encapsulate of reactive compound combination dipping.
These preparations are with the known method preparation, and for example through reactive compound is made up and incremental agent, promptly liquid flux and/or solid carrier mix and produce, optional surfactant, i.e. emulsifier and/or dispersant and/or the blowing agent of using in the preparation.
Under the situation that makes water as incremental agent, for example, also can be with an organic solvent as cosolvent.The liquid flux that is fit to mainly contains: arene, like xylol, toluene or Fluhyzon; Chlorinated aromatic hydrocarbons class or chloro fat hydro carbons are like chlorobenzene class, polyvinyl chloride-base or carrene; Fat hydrocarbon, like cyclohexane or alkane, for example petroleum cuts, mineral oil and vegetable oil; Alcohols, like butanols or ethylene glycol and ether and ester class, ketone is like acetone, methyl ethyl ketone, methyl iso-butyl ketone (MIBK) or cyclohexanone; Intensive polar solvent, like dimethyl formamide and methyl-sulfoxide, and water.
The solid carrier that is fit to has:
For example, ammonium salt and natural minerals powder are like kaolin, clay, talcum, chalk, quartz, Attagel, imvite or diatomite and synthetic mineral powder, like high dispersive silica, aluminium oxide and silicate; The solid carrier that is fit to granule has: for example; The natural rock of pulverizing and classification; Like calcite, marble, float stone, sepiolite and dolomite, and synthetic inorganic and organic dust particle, and the particle of organic material such as sawdust, shuck, corn ears and stems and tobacco stem; The emulsifier and/or the blowing agent that are fit to have: for example nonionic and anion emulsifier; Like polyoxyethylene fatty acid ester, polyoxyethylene aliphatic alcohol ether, for example alkylaryl polyglycol ether, alkylsulfonate, alkyl sulfate, arylsulphonate and protein hydrolysate; The dispersant that is fit to has: for example lignin sulfite waste liquor and methylcellulose.
In preparation, also can use the natural and synthetic polymer of sticker such as carboxymethyl cellulose and powder, particle or latex shape, like gum Arabic, polyvinyl alcohol and polyvinyl acetate, and natural phospholipid such as cephalin and lecithin and synthetic phospholipid.Other additive can be mineral oil and vegetable oil.
Can use colouring agent such as inorganic pigment, for example iron oxide, titanium oxide and Prussia are blue, and organic dyestuff, like the salt of alizarin dyes, azo dyes and metal phthalocyanine dyestuff and trace nutrients such as iron, manganese, boron, copper, cobalt, molybdenum and zinc.
Usually contain 0.1-95% by weight in the preparation, the reactive compound of preferred 0.5-90%.
Reactive compound of the present invention combination can be used as with other reactive compound for example insecticide, attractant, bactericidal agent, bactericide, miticide, nematocide, fungicide, growth regulatory substance or weed killer herbicide mixture and be present in commercial preparation or the type of service by these formulation preparation.Insecticide is particularly including phosphoric acid ester for example, carbamates, carboxylic acid esters, chlorinated hydrocarbon, phenyl ureas with particularly by the material of microorganisms.
The specially suitable instance of the mixed component in mixture is a following compounds:
Fungicide:
Aldimorph, the acid of ammonia propyl-phosphine, ammonia propyl-phosphine acid potassium, Andoprim, anilazine, penta ring azoles, nitrile Fluoxastrobin,
M 9834, benodanil, benomyl, benzyl olefin(e) acid, benzyl olefin(e) acid-isobutyl ester, bilanafos, binapacryl, biphenyl, Bitertanol, blasticidin-S, chaff rhzomorph, the phonetic bacterium spirit of sulphur, buthiobate,
Lime sulfur, Capsimycin, difoltan, captan, carbendazim, carboxin, Carvon, the mite manganese that goes out, the pest of going out azoles, benzene imidazoles bacterium, chloroneb, chloropicrin, tpn, chlozolinate, Clozylacon, cufraneb, cymoxanil, cyproconazole, ring third pyrimidine, cyprofuram
Two ethoxy imidazoles prestige, antiphen, diclobutrazol, Diclofluanid, diclomezine, botran, the mould Wei 、 of second Difenoconazole, Milcurb, dimethomorph, alkene azoles alcohol, alkene azoles alcohol-M, karathane, diphenylamines, pyrrole bacterium sulphur, Plondrel, Delan, dodemorfe, dodine, drazoxolon
Hinosan, oxole bacterium, etaconazole, Milstem, kobam,
Azolactone bacterium, fenapanil, fenarimol, RH-7592, methuroxam, kind clothing ester, fenpiclonil, benzene rust are fixed, butadiene morpholine, fentinacetate, fentin hydroxide, ferbam, ferimzone, fluorine decide amine, fluorine biphenyl bacterium (Flumetover), fluorine bacterium peace, Fluquinconazole, flurprimidol, Flusilazole, flusulfamide, flutolanil, powder azoles amine, folpet, fosetyl (Fosetyl-Aluminium), fosetyl (Fosetyl-Natrium), Rabcide, furidazol, Furalaxyl, the spirit of furan pyrazoles, sterilization pacify (Furcarbonil), furconazole, furconazole_cis, seed dressing amine,
Guazatine,
Hexachloro-benzene, own azoles Chun 、 hymexazo,
IMAZALIL, acid amides azoles, biguanides hot (Iminoctadin), biguanides suffering are to dodecyl benzene sulfonate (Iminoctadinealbesilate), biguanide spicy acid salt, Iodocarb, cycltebuconazole, different oryzon (IBP), different third fixed, iprovalicarb, Irumamycin, Fujione, chlorobenzene Climbazole
Kasugarnycin, imines bacterium, copper product, as, Kocide SD, copper naphthenate, COPPER OXYCHLORIDE 37,5, copper sulphate, copper oxide, copper 8-hydroxyquinolinate and basic copper sulfate mixture,
Copper-manganese mixture, mancozeb, maneb, Meferimzone, mepanipyrim, the third oxygen mebenil, metalaxyl, ring penta azoles bacterium, methasulfocarb, first methuroxam, Carbatene, benzene pyrrole Lip river bacterium (Metomeclam), metsulfovax, midolthromycin, nitrile bacterium azoles, myclozolin
Sankel, different third disappears, nuarimol,
Fenfuram, Wakil, Oxamocarb, oxolinic acide, oxycarboxin (Oxycarboxim), Oxyfenthiin,
Paclobutrazol, pefurazoate, penconazole, Pencycuron, two S-seven, myprozine, pipron, Polyoxin, Polyoxorim, probenazole, Prochloraz, sterilization profit, hundred dimension spirits, Propanosine-Natrium, propiconazole, propineb, Ppyrazophos, pyrifenox, pyrimethanil, pyroquilon, chlorine pyrrole furan ether
Azoles oxolinic acide, pcnb (PCNB),
Sulphur and sulphur preparation,
Tebuconazole, tecloftalam, tecnazene, accent cyclenes, fluorine ether azoles, thiabendazole, thicyofen, thifluzamide, thiophanate methyl, tmtd, sulphur benzonitrile formamide, tolelofos-methyl, tolyfluanid, triazolone, bacterium azoles alcohol, butrizol, azoles bacterium piperazine, poplar bacterium amine, tricyclazole, tridemorph, fluorine bacterium azoles, triforine, triticonazole
Uniconazole P,
Valida, vinclozolin, alkene frost benzyl azoles,
Zarilamid, zineb, ziram and
Miaow grass ester G,
OK-8705,
OK-8801,
α-(1, the 1-dimethyl ethyl)-β-(2-phenoxy group ethyl)-1H-1,2,4-triazole-1-ethanol,
α-(2,4 dichloro benzene base)-β-fluoro-beta-propyl group-1H-1,2,4-triazole-1-ethanol,
α-(2,4 dichloro benzene base)-'beta '-methoxy-Alpha-Methyl-1H-1,2,4-triazole-1-ethanol,
α-(5-methyl isophthalic acid, 3-diox-5-yl)-β-[[4-(trifluoromethyl)-phenyl]-methylene]-1H-1,2,4-triazole-1-ethanol,
(5RS, 6RS)-6-hydroxyl-2,2,7,7-tetramethyl-5-(1H-1,2,4-triazol-1-yl)-3-octanone,
(E)-α-(methoxyimino)-N-methyl-2-phenoxy group-phenyl-acetamides,
2-methyl isophthalic acid-[[[1-(4-aminomethyl phenyl)-ethyl]-amino]-carbonyl]-propyl group)-carbamic acid-1-isopropyl esters,
1-(2,4 dichloro benzene base)-2-(1H-1,2,4-triazol-1-yl)-ethyl ketone-O-(phenyl methyl)-oxime,
1-(2-methyl isophthalic acid-naphthyl)-1H-pyrroles-2, the 5-diketone,
1-(3, the 5-dichlorophenyl)-3-(2-acrylic)-2, the 5-pyrrolidine-diones,
1-[(diiodomethyl)-sulfonyl]-4-methyl-benzene,
1-[[2-(2, the 4-difluorophenyl)-1,3-dioxolanes-2-yl]-methyl]-1H-imidazoles,
1-[[2-(4-chlorphenyl)-3-phenyl ethylene oxide base]-methyl]-1H-1,2, the 4-triazole,
1-[1-[2-[(2,4 dichloro benzene base)-methoxyl group]-phenyl]-vinyl]-1H-imidazoles,
1-methyl-5-nonyl-2-(phenyl methyl)-3-pyrrolidinol (pyrrolidinol),
2 ', 6 '-two bromo-2-methyl-4 '-trifluoromethoxy-4 '-Trifluoromethyl-1,3-thiazole-5-formailide (carboxanilid),
2,2-two chloro-N-[1-(4-chlorphenyl)-ethyl]-1-ethyl-3-methyl cyclopropane formamide,
2,6-two chloro-5-(methyl sulfenyl)-4-pyrimidine radicals thiocyanates,
2,6-diamino-N-(4-trifluoromethyl benzyl)-benzamide,
2,6-two chloro-N-[[4-(trifluoromethyl)-phenyl]-methyl]-benzamide,
2-(2,3,3-three iodo-2-acrylic)-2H-tetrazolium,
2-[(1-Methylethyl)-sulfonyl]-5-(trichloromethyl)-1,3, the 4-thiadiazoles,
2-[[6-deoxidation-4-O-(4-O-methyl-β-D-glucopyranosido)-a-D-glycopyranosyl]-amino]-4-methoxyl group-1H-pyrrolo-[2,3-d] pyrimidine-5-nitrile,
The 2-butylamine,
2-bromo-2-(bromomethyl)-pentane dintrile,
2-fluoro-N-(2,3-dihydro-1,1,3-trimethyl-1H-indenes-4-yl)-3-pyridine carboxamide
2-chloro-N-(2, the 6-3,5-dimethylphenyl)-N-(isothiocyanato methyl)-acetamide,
2-phenylphenol (OPP),
3,4-two chloro-1-[4-(difluoro-methoxy)-phenyl]-1H-pyrroles-2, the 5-diketone,
3,5-two chloro-N-[cyanic acid [(1-methyl-2-propynyl)-oxygen base]-methyl]-benzamide,
3-(1,1-dimethyl propyl-1-oxo)-1H-indenes-2-nitrile,
3-[2-(4-chlorphenyl)-5-ethyoxyl-3-isoxazole alkyl]-pyridine,
4-chloro-2-cyanic acid-N, N-dimethyl-5-(4-aminomethyl phenyl)-1H-imidazoles-1-sulfonamide,
4-methyl-tetrazolo [1,5-a] quinazoline-5 (4H)-ketone,
8-(1, the 1-dimethyl ethyl)-N-ethyl-N-propyl group-1,4-dioxo spiro [4.5] decane-2-methylamine,
Oxine sulphate,
9H-xanthene-9-formic acid-2-[(phenyl amino)-carbonyl]-hydrazides,
Two-(1-Methylethyl)-3-methyl-4-[(3-methyl benzoyl)-oxygen bases]-2,5-thiophene dicarboxylic acid esters,
Suitable-1-(4-chlorphenyl)-2-(1H-1,2,4-triazol-1-yl)-suberol,
Suitable-4-[3-[4-(1, the 1-dimethyl propyl)-phenyl-2-methyl-propyl]-2,6-dimethyl-morpholine hydrochloride,
[(4-chlorphenyl)-azo]-cyan-acetic ester,
Saleratus,
Methane four mercaptan sodium salts,
1-(2,3-dihydro-2,2-dimethyl-1H-indenes-1-yl)-1H-imidazoles-5-methyl formate,
N-(2, the 6-3,5-dimethylphenyl)-N-(5-isoxazolyl carbonyl)-DL-methyl lactamine,
N-(chloracetyl)-N-(2, the 6-3,5-dimethylphenyl)-DL-methyl lactamine,
N-(2,3-two chloro-4-hydroxy phenyls)-1-methyl-cyclohexyl alkane formamide,
N-(2, the 6-3,5-dimethylphenyl)-2-methoxyl group-N-(tetrahydrochysene-2-oxo-3-furyl)-acetamide,
N-(2, the 6-3,5-dimethylphenyl)-2-methoxyl group-N-(tetrahydrochysene-2-oxo-3-thienyl)-acetamide,
N-(2-chloro-4-nitrobenzophenone)-4-methyl-3-nitro-benzsulfamide,
N-(4-cyclohexyl phenyl)-1,4,5,6-tetrahydrochysene-2-pyrilamine,
N-(4-hexyl phenyl)-1,4,5,6-tetrahydrochysene-2-pyrilamine,
N-(5-chloro-2-aminomethyl phenyl)-2-methoxyl group-N-(2-oxo-3-oxazole alkyl)-acetamide,
N-(6-methoxyl group)-3-pyridine radicals)-cyclopropane carboxamide,
N-[2,2,2-three chloro-1-[(chloracetyl)-amino]-ethyl]-benzamide,
N-[3-chloro-4, two (2-propynyl oxygen the base)-phenyl of 5-]-N '-methoxyl group-first Imidamide (methanimidamid),
N-formoxyl-N-hydroxyl-DL-alanine-sodium salt,
[2-(dipropyl is amino)-2-oxoethyl]-ethylenebis dithiocarbamate phosphoramidic acid O, O-diethyl ester (ethylphosphoramidothioat)
Phenyl propyl sulfo-amino phosphoric acid O-methyl S-phenylester,
1,2,3-diazosulfide-7-carbothioic acid S-methyl esters,
Spiral shell [2H]-1-chromene-2,1 ' (3 ' H)-isobenzofuran]-3 '-ketone,
Bactericide:
Bronopol, antiphen, N-Serve, Sankel, kasugarnycin, different thiophene bacterium ketone, furancarboxylic acid, terramycin, probenazole, streptomycin, tecloftalam, copper sulphate and other copper agent.
Insecticide/miticide/nematocide:
AVM, orthene, Acetamiprid, acrinathrin, alanycarb, Aldicarb, aldoxycarb, nail body flucythrinate (Alphacypermethrin), nail body cypermethrin (Alphamethrin), Amitraz, Olivomitecidin, AZ 60541, Ai Zhading, azamethiphos, azinphos-methyl A, azinphos-methyl M, azacyclotin
Bacillus popilliae, Bacillus sphaericus, Ke oppose gram bacterium, Su Jin bacillus, Baculoviruses, Beauveria bassiana, Beauveria tenella, Ficam, Benfuracard micro, bensultap, Citrazon, β-fluvalinate, Bifenazate, Biphenthrin, Bioethanomethrin, biological ammonia chrysanthemum ester, BPMC, bromophos A, metalkamate, Buprofezin, special Pyrimitate, butocarboxim, butyl pyridaben (Butylpyridaben),
Cadusafos, carbaryl, carbofuran, trithion, carbosulfan, cartap, Chloethocarb, chlorethoxyfos, fluorine azoles worm are clear, chlorfenviphos, fluorine pyridine urea, chlormephos, chlopyrifos, chlopyrifos M, Chlovaporthrin, cis Chryson (Cis-Resmethrin), Cispermethrin, Clocythrin, remove line one-tenth, four mite piperazines, cynock, Cycloprene, cycloprothrin, cyfloxylate, cyhalothrin, plictran, cypermethrin, fly eradication amine
Decis, demeton M, demeton S, demeton-methyl, butyl ether urea, diazinon, dichlorvos, kelthane, Rogor, dimethylvinphos, Dinotefuran, difenolan, disulfoton, iodoxy fourth two sufferings, benzene oxycetylene mite,
Eflusilanate, Emamectin, empenthrin, 5a,6,9,9a-hexahydro-6,9-methano-2,4, Entomopfthoraspp., esfenvalerate, benzene worm prestige, ethion, Ethiprole, ethoprop, ether chrysanthemum ester, Te Ben oxazole, oxygen Diothyl,
Nemacur, fenazaquin, fenbutatin oxide, sumithion, fenothiocarb, Fenoxacrim, ABG-6215, fenpropathrin, Fenpyrad, Fenpyrithrin, azoles mite ester, kill chrysanthemum ester, sharp strength spy, fluazinam, fluorine fluazuron, Flubrocythrinate, flucycloxuron, flucythrinate, flufenoxuron, Flutenzine, taufluvalinate, Dyfonate, fosmethilan, thiazolone phosphorus, Fubfenprox, furathiocarb
Granulosis virus,
Benzoic acid N-tert-butyl-N-(4-chlorobenzoyl)hydrazide, HCH, heptan worm phosphorus, fluorine bell urea, Hexythiazox, hydroprene,
Imidacloprid 、 oxadiazole worm, isazofos, propylamine phosphorus 、 karphos, Olivomitecidin,
Nucleopolyhedrosis virus,
λ-cyhalothrin, the fluorine third oxygen urea,
Malathion, Afos, the methaldehyde, acephatemet, Metharhiziumanisopliae, Metharhizium flavoviride, methidathion, mercaptodimethur, methomyl, Runner, MTMC, metoxadiazone, Menite, milbemycin, Azodrin
2-dichloroethylk dimethyl phosphate, nitenpyram, Nithiazine, Rimon,
Omethoate, methylamine fork prestige, metilomerkaptofosoksid,
Paecilomyces fumosoroseus, parathion A, parathion-methyl, permethrin, phenthoate dimephenthoate cidial, thimet, zolone, phosmet, phosphamidon, phoxim, Aphox, Actellic A, methyl Actellic, Profenofos, propargite, Carbamult, unden, Toyodan, Fac, pymetrozine, pyraclofos, anti-Chryson, Dalmatian chrysanthemum, pyridaben, pyridathion, pyramine phenylate, pyriproxyfen
Quinalphos,
Ribavirin,
Salithion, cadusafos, deinsectization silicon ether, SPINOSYN, Spirodiclofen, Spiromesifen, sulfotep, second Toyodan,
Taufluvalinate; RH-5992; Tebufenpyrad; Tebupirimphos (Tebupirimiphos); Flufenoxuron; Tefluthrin; Swebate; Mercaptodimethur; Terbufos; Tetrachlorvinphos; Tetradiphon; Hot body cypermethrin; Thiophene worm quinoline (Thiacloprid); Thiamethoxam; The moth fly nitrile; Thiatriphos; Thiocyclarn; The two prestige of sulphur; Thiofanox; Enemy Bei Te; Tralocythrin; Tralomethrin; Triarathene; The azoles aphid becomes; Hostathion; Triazuron; Trichlophenidine; Chlorophos; Desinsection is grand; Landrin
Kilval, fluorine pyrazoles worm, Verticillium lecani,
YI?5302,
Zeta-cypermethrin、Zolaprofos,
3-[(dihydro-2-oxo--3 (2H) furans subunit)-methyl]-2,2-dinethyl cyclopropane carboxylic acid (1R-is suitable)-[5-(phenyl methyl)-3-furyl]-methyl ester,
2,2,3,3-tetramethyl cyclopropane-carboxylic acid [(3-Phenoxyphenyl)-methyl] ester,
1-[(2-chloro-5-thiazolyl) methyl] tetrahydrochysene-3,5-dimethyl-N-nitro-1,3,5-triazines-2 (1H)-imines,
2-(2-chloro-6-fluorophenyl)-4-[4-(1, the 1-dimethyl ethyl) phenyl]-4,5-dihydro-oxazoles,
2-(acetyl group oxygen base)-3-dodecyl-1, the 4-naphthalenedione,
2-chloro-N-[[[4-(1-phenyl ethoxy)-phenyl]-amino]-carbonyl]-benzamide,
2-chloro-N-[[[4-(2,2-diamino-1,1-difluoroethoxy)-phenyl]-amino]-carbonyl] benzamide,
Propyl carbamic acid (3-aminomethyl phenyl) ester,
4-[4-(4-ethoxyl phenenyl)-4-methyl amyl]-1-fluoro-2-phenoxy group-benzene,
4-chloro-2-(1, the 1-dimethyl ethyl)-5-[[2-(2,6-dimethyl-4-phenoxy group phenoxy group) ethyl] sulfenyl]-3 (2H)-pyridazinones,
4-chloro-2-(2-chloro-2-methyl-propyl)-5-[(6-iodo-3-pyridine radicals) methoxyl group]-3 (2H)-pyridazinones,
4-chloro-5-[(6-chloro-3-pyridine radicals) methoxyl group]-2-(3, the 4-dichlorophenyl)-3 (2H)-pyridazinones,
Bacillus thuringiensis strains EG-2348,
Benzoic acid [2-benzoyl-1-(1, the 1-dimethyl ethyl)-hydrazides,
Butyric acid [2,2-dimethyl-3-(2,4 dichloro benzene base)-2-oxo-1-oxaspiro [4.5] last of the ten Heavenly stems-3-alkene-4-yl] ester,
[3-[(6-chloro-3-pyridine radicals) methyl]-2-thiazolidine subunit]-cyanamide,
Dihydro-2-(Nitromethylene)-2H-1,3-thiazine-3 (4H)-formaldehyde,
[2-[[1,6-dihydro-6-oxo-1-(phenyl methyl)-4-pyridazinyl] oxygen base] ethyl]-urethanes,
N-(3,4,4-three fluoro-1-oxo-3-cyclobutenyls)-glycine,
N-(4-chlorphenyl)-3-[4-(difluoro-methoxy) phenyl]-4,5-dihydro-4-phenyl-1H-pyrazoles-1-formamide,
N-methyl-N '-(1-methyl-2-acrylic)-1,2-hydrazine two thioformamides,
N-methyl-N '-2-acrylic-1,2-hydrazine two thioformamides,
[2-(dipropyl is amino)-2-oxoethyl]-ethylenebis dithiocarbamate phosphoramidic acid O, the O-diethyl ester.
With other known activity compound for example the mixture of weed killer herbicide or fertilizer and growth regulator also be possible.
When the insecticide, reactive compound combination of the present invention can also exist with its commercial preparation with by the form of the mixture of the application form of above-mentioned formulation preparation and synergist.Synergist is to increase the active compound of reactive compound, but the synergist itself that adds is not must be activated.
Content by reactive compound in the application form of commercial preparation preparation can change in very wide scope.The concentration of reactive compound is 0.0000001-95 weight % reactive compound, preferred 0.0001-1 weight % in the type of service.
Said compound uses with the conventional method that is applicable to application form.
When being used to prevent and treat sanitary insect pest and the control of insect of warehousing product, reactive compound of the present invention combination has good timber and clay residual activity and the substrate that is brushed with lime is had good alkaline stability.
Reactive compound combination of the present invention not only has activity to the insect in plant insect, sanitary insect pest and the stored goods; And in veterinary applications; Controlling animal parasites (epizoa) also there is activity, for example hard tick, soft ticks, mange mite, lice shape Pu mite, fly (bite and suck), parasitism fly larva, lice, hair lice, poultry louse and flea.These parasites comprise:
Anoplura, for example, Haematopinus, jaw lice genus, lice genus, Phtirus spp. and pipe lice belong to;
Mallophaga and Amblycera and thin angle suborder, for example, hair Trichodectes, Menoponspp., huge Linognathus, Trichodectes, Werneckiella spp., Lepikentron spp., Damalinia, Trichodectes and Felicola;
Diptera and Nematocera and Brachycera; For example, Aedes, Anopheles, Culex, Simulium, Eusimulium, owl midge, Lutzomyia spp., Bitting midge, Chrysops, knurl Gadfly, Atylotus, Gadfly, Chrysozona, Philipomyia spp., honeybee Hippobosca., Musca, Hydrotaea, Genus Stomoxys, horn fly belong to, not fly genus, Fannia, Glossina, Calliphora, Lucilia, Carysomyia, Wohlfahrtia spp., Sarcophaga, Oestrus, Hypoderma, Gasterophilus, Hippobosca, Lipoptena spp. and Melophagus;
Siphonaptera, for example, flea genus, Ctenocephalus, Xanthopsyllacheopis belong to and Ceratophyllus;
Heteroptera, for example, Cimex, vertebra Reduvius, red abdomen Reduvius and Panstrongylus;
Blattaria, for example, oriental cockroach, American cockroach, Groton bug and blattaria belong to;
Acarina and back valve suborder and Mesostigmata; For example, Argas, Ornithodorus, residual beak tick genus, hard tick genus, Amblyomma, Boophilus, Dermacentor, Haemophysalis spp., Hyalomma, Rh, Dermanyssus, the sharp mite genus of thorn, Pneumonyssus, Sternostoma and Varroa;
Spoke mite suborder (preceding valve suborder) and flour mite order (Astigmata); For example, the honeybee tarsonemid belongs to, a Ji stings the mite genus, fowl stings a li mite genus, Myobia, Psorergates, Demodex, Trombidium, yak mite genus, Tyroglyphus, Tyrophagus, have a liking for mite genus, wing mite genus, scabies mite genus, Psoroptes, Notoedres, itch mite genus, scab mite genus, lump mite genus, Cytoleichus and epithelium mite genus under wooden mite genus, the neck.
Reactive compound combination of the present invention also is applicable to the arthropods of control invasion agricultural production property domestic animal; Said agriculture domestic animal such as ox, sheep, goat, horse, pig, donkey, camel, buffalo, rabbit, chicken, turkey, duck, goose and honeybee; Other domestic pets; For example the fish in dog, cat, the bird of raising in cages, aquarium also has so-called experimental animal, for example vole, cavy, rat and mouse.Through preventing and treating above-mentioned arthropods, should be able to reduce the situation of the animal dead and the underproduction (meat, milk, hair, skin, egg, honey etc.), therefore, the application of the invention reactive compound can make the livestock breeding management more economical and easy.
When being applied to veterinary applications, reactive compound combination of the present invention can be through known method promptly through enteral administration, for example with form administrations such as tablet, capsule, potus, filled medicament, granule, paste, bolus, feeding method, suppositorys; Non-through enteral administration, for example through injection (intramuscular injection, hypodermic injection, intravenous injection, intraperitoneal injection etc.), implantation administration; Nose administration; Through percutaneous drug delivery, for example with immersion or dipping, spraying, sprinkle and water, wipe, scrub and the administration of dusting mode, also can be by means of the moulded products that contains reactive compound, for example administrations such as necklace, ear pendant thing, tailpiece thing, limb ring (band), halter, decorative device.
When being used for domestic animal, poultry, pet etc.; Can be as the dosage form (for example pulvis, emulsion, free flowing composition) of the reactive compound that contains 1-80 weight % directly or 100-10 with reactive compound; Use after 000 times of dilution, or it can be used as chemical bath.
In addition, find that reactive compound combination of the present invention also has very strong insecticidal activity to the insect that damages industrial materials.
List following insect as an example and preferably, but be not limited to this:
Coleopteron, as
The North America house longhorn beetle; Green brave longicorn (Chlorophorus pilosis); The furniture death watch beetle; Report dead material death watch beetle; Class wing death watch beetle; Dendrobium pertinex; Pine bud branch death watch beetle; Pine product death watch beetle (Priobium carpini); Lyctus brunneus Stephens; Powder moth-eaten (Lyctus africanus); The south powder is moth-eaten; Quercitron is moth-eaten; Powder moth-eaten (Lyctus pubescens); Chest powder moth-eaten (Trogoxylonaequale); Minthea rugicollis; The material bark beetle belongs to; The wood strip bark beetle belongs to; Coffee is black long moth-eaten; Bostrychuscapucins; Brown different wing is long moth-eaten; Long moth-eaten genus of sour jujube and bamboo pole powder are long moth-eaten.
Dermaptera, for example
Blue-black wood wasp, the big wood wasp of dragon spruce, safe increasing wood wasp and big wood wasp (Urocerus augur).
Termite, for example
Kalotermitid (Kalotermes flavicollis), a fiber crops heap sand termite, the different termite of Indian-Pakistani structural wood, American-European reticulitermes flavipe, reticulitermes flavipe (Reticulitermes santonensis), reticulitermes flavipe (Reticulitermes lucifugus), Darwin Australia termite, the ancient termite in Nevada and Taiwan formosanes.
Thysanoptera, for example Taiwan silverfish.
Industrial materials on the meaning of the present invention are appreciated that and are the expression non-living material, the wooden article and the coating composition of for example preferred plastics, adhesive, glue, paper and plate, leather, timber, processing.
The wooden article of timber and processing is to need preferred protection to make it avoid the material of insect infestations especially.
Available activating agent of the present invention or the timber and the wooden article of processing that contain their mixture protection are appreciated that to be to represent, for example:
Building timber, wooden frame, railroad sleeper, bridge module, bridge type harbour, the wooden vehicles, chest, shelf, container, phone mast, wooden outer cover, timber window and timber, plywood, chipboard, in building construction or construction joiner industry joiner or wooden article commonly used.
Reactive compound combination of the present invention can be direct, or with conc forms or conventional formulation, use like pulvis, granule, solution, suspending agent, emulsion or paste mode.
Above-mentioned preparation can known method own prepare; For example through reactive compound and at least a solvent or thinner, emulsifier, dispersant and/or adhesive or fixative, water repellent agent are mixed; And as need to add drier and UV stabilizing agent and as need add dyestuff and pigment and other processing aid.
The Pesticidal combination or the concentrate of the goods that are used for protecting timber and derived by timber comprise that concentration is 0.0001 to 95% weight %, particularly the reactive compound of the present invention of 0.001 to 60 weight %.
The usage amount of composition or concentrate is according to the kind of insect and existence and medium and definite.The optimal application rate can be confirmed through campaign when using separately.Yet the material based on the need protection uses 0.0001 to 20 weight % usually, and the reactive compound of preferred 0.001 to 10 weight % is enough.
Used solvent and/or thinner are oiliness or oils organic chemistry solvent or solvent mixture and/or polar organic solvent or the solvent mixture and/or the water of organic chemistry solvent or solvent mixture and/or low volatility, can add emulsifier and/or wetting agent like needs.
The preferred organic chemistry solvent that uses is oiliness or oils solvent, its evaporation number greater than 35 and flash-point greater than 30 ℃, and be preferably greater than 45 ℃.Being used as above-mentioned low volatility and water-fast oiliness and oils vehicle substance is corresponding mineral oil or their aromatic fraction, or contains the solvent mixture of mineral oil, preferred petroleum solvent, oil and/or alkylbenzene.
The preferred boiling range of using is 250-350 ℃ bobbin oil and boiling range oil or the aromatic hydrocarbons as 160-280 ℃ as 170-220 ℃ mineral oil, boiling range as 170-220 ℃ petroleum solvent, boiling range, and the turpentine wet goods.
In a preferred embodiment, use boiling range to be 180-220 ℃ the aromatics and high boiling range mixture and/or the bobbin oil and/or the naphthalene monochloride of aliphatic hydrocarbon, preferred α-naphthalene monochloride as 180-210 ℃ liquid aliphatic hydrocarbon or boiling range.
Evaporation number greater than 35 and flash-point partly replace greater than 30 ℃ and the organic oiliness or the organic chemistry solvent that the oils solvent can be used volatile or middle volatility that are preferably greater than 45 ℃ low volatility; Condition be solvent mixture evaporation number equally greater than 35 and flash-point greater than 30 ℃ and be preferably greater than 45 ℃, and this insecticide/bactericides mixture is solvable maybe can be emulsifiable in the above-mentioned solvent mixture.
In preferred embodiments, some organic chemistry solvent or solvent mixture are substituted by aliphatic polar organic solvent or solvent mixture.The preferred aliphatic organic chemistry solvent that contains hydroxyl and/or ester group and/or ether, for example glycol ethers, the ester etc. of using.
The organic chemistry adhesive that the present invention uses is synthetic resin and/or bonding drying oil; Their itself known dilutable water and/or solubilized or dispersion or be emulsifiable in the organic chemistry solvent of above-mentioned use; Particularly by following material adhesive that form or that comprise following material: acrylic resin, vinylite; The for example alkyd resins of polyvinyl acetate, polyester resin, polycondensation or polyaddition resin, polyurethane resin, alkyd resins or modification, phenolic resins, hydrocarbon resins are like indene-coumarone resin, organic siliconresin, dry vegetable oil and/or drying oil and/or based on the physics dry adhesive of natural and/or synthetic resin.
As the synthetic resin of adhesive can emulsion, dispersant or solution form use.Pitch or asphaltic substances also can be used as adhesive, and consumption is at most 10 weight %.Can also known dyestuff, pigment, waterproofing agent, smell conditioning agent and inhibitor or the preservative etc. of use itself.
In the present composition or concentrate, preferably include at least a alkyd resins or modified alkyd resin and/or dry vegetable oil as the organic chemistry adhesive.The present invention preferably uses oil content greater than 45 weight %, the alkyd resins of preferred 50-68 weight %.
Can all or part ofly be fixed agent (mixture) or plasticizer (mixture) of above-mentioned adhesive substitutes.The purpose that adds these additives is evaporation and crystallization or the deposition that prevents reactive compound.They preferably substitute 0.01 to 30% adhesive (adhesive to use is 100%).
Plasticizer is selected from the chemical substance of phthalate, like dibutyl phthalate, dioctyl phthalate or benzyl butyl phthalate; Phosphoric acid ester such as tributyl phosphate; Adipate ester is like two-(2-ethylhexyl) adipate esters; Stearate is like butyl stearate or amyl stearate; Oleate is like butyl oleate; The glycol ethers of glycerin ether or higher molecular weight; Glyceride and p-toluenesulfonic esters.
Fixative is chemically based on the polyethylene alkyl ethers, like polyvinyl methyl ether or ketone, like benzophenone and ethylene Benzophenone.
Solvent that other is suitable for or thinner be water particularly, and conduct is used with the mixture of one or more above-mentioned organic chemistry solvents or thinner, emulsifier and dispersant if desired.
Especially effectively the wood protection method is through large batch of dipping method, for example reaches through vacuum, two vacuum or pressure method.
The existing insecticide and one or more optional fungicides that comprises other of also can choosing wantonly with composition.
Reactive compound combination of the present invention can be used for protecting the various article, particularly hull, filter, net, Ship Structure, anchor and the recoil simulator that often contact with seawater or salt solution to avoid biological attachment.
Because settling down property Oligochaeta order; Like Serpulidae and shell-fish and Ledamorpha (Lepas) class; Belong to and armour tender tea leaves lotus genus like various tender tea leaves lotuses; Or Balanomorpha (barnacle worm), like Balanus or refer to that the tender tea leaves lotus belongs to adhere to the frictional resistance that has increased hull and owing to increased energy resource consumption and often be detained dry dock in addition, the obvious like this operation cost that increased.
Aufwuch also has marine alga in addition, and for example Ectocarpus and Ceramium it is especially important the adhering to of settling down property Malacostraca (Entomostraca) that this Entomostraca is included in the cirrus guiding principle (cirrus class crustacean).
Astoundingly, have now found that reactive compound combination of the present invention has outstanding antifouling (anti-adhering to) effect.
The reactive compound combination of the application of the invention; Can not use heavy metal; As; For example vulcanize two (trialkyltins), lauric acid tri-n-butyl tin, oxidation tri-n-butyl tin, cuprous oxide (I), triethyltin chloride, three normal-butyls (2-phenyl-4-chlorophenoxy)-Xi, tributyltin oxide, molybdenum bisuphide, antimony oxide, polymerization butyl titanate, phenyl-(bipyridyl)-bismuth chloride, the zinc of fluoridizing tri-n-butyl tin, ethylene thiocarbamic acid manganese, PZ, ethylenebis thiocarbamic acid zinc, 2-pyridinethiol-1-oxide and mantoquita, two DMDS for carbamoyl ethylenebis thiocarbamic acid zinc, zinc oxide, ethylenebis aminodithioformic acid cuprous (I), cupric thiocyanate, copper naphthenate and halogenation tributyl tin, or significantly reduce above-claimed cpd concentration.
Promptly also can choose wantonly and comprise other reactive compound, preferred algicide, fungicide, weed killer herbicide, invertebrate poison or other antifouling activity compound with anti-fouling paint.
Following component is preferred for the blending ingredients of antifouling composition of the present invention:
Algicide, as
2-tert-butyl group amino-4-cyclopropyl amino-6-methyl mercapto-1,3,5-triazines, antiphen, diuron, endothall, fentinacetate, isoproturon, methabenz thiazuron, Oxyfluorfen, quinoclamine and terbutryn,
Fungicide, as
Benzo [b] thiophenic acid cyclohexyl amide-S; S-dioxide, Euparen, Fluorfolpet, 3-iodo-2-propynyl butyl carbamate, tolyfluanid and azole are like penta ring azoles, cyproconazole, oxole bacterium, own azoles alcohol, ring penta azoles bacterium, propiconazole and Tebuconazole;
Invertebrate poison, as
Fe-chelating agent fentinacetate, the methaldehyde, mercaptodimethur, niclosamide, the two prestige of sulphur and Landrin;
Or antifouling activity compound commonly used, as
4,5-two chloro-2-octyl groups-4-isothiazoline-3-ketone, diiodomethyl paratryl sulfone, 2-(N, N-dimethyl thiocarbamoyl sulfenyl)-5-nitrothiazole base, potassium, copper, sodium and the zinc salt of 2-pyridinethiol-1-oxide, pyridine triphenylborane, tetrabutyl distannoxane, 2; 3,5,6-tetrachloro-4-(mesyl)-pyridine, 2; 4,5,6-daconil M, tetramethylthiuram disulfide and 2; 4,6-trichlorophenyl maleimide.
Comprising concentration in the antifouling composition that uses is 0.001 to 50 weight %, particularly the reactive compound of the present invention of 0.01 to 20 weight %.
Antifouling composition of the present invention also is included in for example Ungerer of following document, Chem.Ind.1985,37,730-732 and Williams, Antifouling MarineCoatings, Noyes, Park Ridge, disclosed usual component in 1973.
Except killing algae, antifungal, kill mollusk reactive compound and the insecticidal active compound of the present invention, in the antifouling paint compositions also particularly including adhesive.
The instance of known adhesive comprises polyvinyl chloride in the dicyandiamide solution, the chlorinated rubber in the dicyandiamide solution, dicyandiamide solution particularly vinyl chloride/vinyl acetate co-polymer system, Butadiene/acrylic-nitrile rubber, the drying oil of acrylic resin, aqueous dispersion form or the organic solvent system form in the Aquo System; Like Linseed oil, resin ester or mix the modification animi resin that forms with tar or pitch, pitch and epoxide, a spot of chlorinated rubber, chlorinated polypropylene and vinylite.
Also choose wantonly in the coating composition and can comprise inorganic pigment, organic pigment or the dyestuff that preferably is insoluble to salt solution.Also can comprise like the rosin based material, so that reactive compound controllably discharges in the coating composition.In addition, can comprise plasticizer in the coating, influence the modifying agent of the rheological equationm of state, and other conventional component.Can also the The compounds of this invention combination be added in the polishing antifouling system.
Reactive compound of the present invention also is suitable for preventing and treating enclosure space, like animal pest, particularly insect, mite class and the spider of taking place in the spaces such as apartment, factory building, office, compartment.They itself or make up and to use through being added into the domestic pesticide product that is used for preventing and treating above-mentioned insect with other reactive compound and auxiliary agent.They all have insecticidal activity to responsive and resistant population and all developmental stage.These insects comprise:
Scorpionida for example clamps scorpion (Buthus occitanus).
Acarina, for example adobe tick, stick up edge sharp-edged tick, Bryobia, Dermanyssus gallinae, the sweet mite of family's food, tampan tick, brown dog tick, trombiculid (Trombicula alfreddugesi), Neutrombicula autumnalis, dermatophagoides pteronyssinus and dust mite.
Spider shape order, for example cockle spider section and epeira section.
Opiliones is for example intended scorpion class (Pseudoscorpiones chelifer), Pseudoscorpiones cheiridium and Opiliones phalangium.
Isopoda, for example damp worm and pillworm.
Doubly sufficient order is for example had zebra land and a mountain cricket Eimeria.
Lip foot order, for example DIWUGONG belongs to.
Zygentoma order, for example comb silverfish genus, Taiwan silverfish and Lepismodesinquilinus.
Blattaria, for example oriental cockroach, Groton bug, Blatella (Blattellaasahinai), Ma Dela blattaria, angle abdomen Lian genus, wooden Lian genus, Australian cockroach, American cockroach, the big Lian of foxiness, Peroplaneta fluligginosa and long palpus blattaria.
Saltatoria, for example tame Shuai.
Dermaptera, for example European earwig.
Isoptera, for example kalotermitid belongs to and Reticulitermes.
Corrodentia, for example Lepinatus belongs to and powder corrodent belongs to.
Coleoptera, for example Anthrenus, the moth-eaten genus of fur, khapra beetle genus, a long lesser grain borer, latent instep cuckoo Eimeria, Ptinus, lesser grain borer, grain weevil, rice weevil, corn weevil and Stegobium paniceum.
Diptera, for example Aedes aegypti, aedes albopictus, Aedes taeniorhynchus, Anopheles, calliphora erythrocephala, great number fiber crops horsefly, Culex quinquefasciatus, northern house, Culex tarsalis, Drosophila, Fannia canicularis, housefly, owl midge, sarcophagid (Sarcophaga carnaria), Simulium, tatukira and daddy-longlegs (Tipula paludosa).
Lepidoptera, for example lesser wax-moth, galleria mellonella waxmoth, the ancient phycitid of India, rain moth, bag rain moth and curtain rain moth.
Siphonaptera, for example ctenocephalides canis, ctenocephalides felis nominate subspecies, Pulex irritans, chigo and Xanthopsyllacheopis.
Hymenoptera for example blazons hunchbacked ant, bright hair ant, black wool ant, Lasius umbratus, MonomoriumMayr, Paravespula genus and Pavement Ant.
Anoplura, for example head louse, body louse and crab louse.
Heteroptera, for example cimex hemipterus, bed bug, phodnius prolixus and invasion triatomid.
In the family expenses field of pesticides, its use through they itself or with other suitable activity compound, unite like the reactive compound of phosphoric acid ester, carbamates, pyrethroid, growth regulator class or other known insecticides class and to carry out.
They can be like following use: aerosol; Non pressurized spray, for example pump spraying, spray spraying, fogger, thick fog, foam, gel, have evaporation product, liquid evaporator, gel and the thin film evaporator of the evaporating plate that cellulose or polymer process, pusher evaporator, not energy requirement or passive type vapo(u)rization system, catch moth paper, catch moth bag and insect-catching glue, as granule or pulvis, in spreading bait or the bait position.
When using reactive compound of the present invention to make up, according to application type, rate of application can change in relative broad range.When handling plant part, the rate of application of reactive compound combination of the present invention is generally 0.1-10000g/ha, is preferably 10-1000g/ha.
From the following example, can be clear that the good desinsection and the acaricidal activity of reactive compound combination of the present invention.Though single reactive compound shows weak activity, its combination have surpass active simply add and activity.
When the activity of reactive compound combination surpasses the summation of the activity of reactive compound when using separately, just there are insecticide and acaricidal synergy all the time.
Be used to calculate the formula of synergistic activity of the combination of two kinds of reactive compounds
For the combination of two kinds of given reactive compounds, the activity of expectation can be described below calculating (referring to Carpenter, C.S.; " mammalian toxicity of 1 naphthyl N methyl carbamate [Sevin insecticide] "; Agricultural and Food Chemistry, Vol.9, No.1; The 30-39 page or leaf, 1961):
If Pa is the ratio of reactive compound A in mixture,
Pb is the ratio of reactive compound B in mixture,
LC 50 (or 95)A has 50% (or 95%) concentration when being killed when the animal of handling with reactive compound A, and
LC 50 (or 95)B has 50% (or 95%) concentration when being killed when the animal of handling with reactive compound B, then
Figure S061A0199020060720D000211
Figure S061A0199020060720D000212
If the LC that calculates 50 (or 95)Surpass the actual value that obtains, and be higher than confidence interval, then the activity of combination is to surpass stack, promptly has synergy.
Embodiment
The application implementation example
Embodiment A
Cotton bollworm (Heliothis armigera) test
Solvent: 7 weight portion dimethyl formamides
Emulsifier: the alkylaryl polyglycol ether of 2 weight portions
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Soybean spray (Glycine max) through handling in the active agent preparations that immerses desired concn, and is put cotton bollworm (Heliothis armigera) caterpillar when the soybean page or leaf is still moist.
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in Carpenter formula (see and go up page or leaf), to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table A
Destroy the insect of plant
The cotton bollworm test
Figure S061A0199020060720D000231
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment B
Knurl volume Aphis (Myzus) test
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling the cabbage leaves (Brassica oleracea) of severe infections black peach aphid (Myzus persicae) in the active agent preparations that immerses desired concn.
Behind required time, measure the kill ratio of representing with %.Wherein 100% all aphids of expression all are killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table B
Destroy the insect of plant
The test of knurl volume Aphis
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment C
Plutella (Plutella) test, the responsive system of planting
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, the put diamond-back moth caterpillar of (Plutellaxylostella, the responsive system of planting).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table C
Destroy the insect of plant
The Plutella test, the responsive system of planting
Figure S061A0199020060720D000251
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment D
The test of daikon leaf beetle (Phaedon) larva
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, put the larva of the chrysomelid worm of horseradish ape (Phaedoncochleariae).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all mealworms of expression all are killed; 0% expression does not have mealworm to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table D
Destroy the insect of plant
The test of daikon leaf beetle (Phaedon) larva
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment E
Noctuid (Spodoptera frugiperda) test is coveted on the meadow
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, put the caterpillar of mythimna separata (noctuid is coveted on the meadow).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table E
Destroy the insect of plant
The greedy noctuid test in meadow
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment F
Cotton bollworm (Heliothis armigera) test
Solvent: 7 weight portion dimethyl formamides
Emulsifier: the alkylaryl polyglycol ether of 2 weight portions
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Soybean spray (Glycine max) through handling in the active agent preparations that immerses desired concn, and is put cotton bollworm (Heliothis armigera) caterpillar when Soybean Leaves is still moist.
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table F
Destroy the insect of plant
The cotton bollworm test
Figure S061A0199020060720D000281
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment G
The test of daikon leaf beetle (Phaedon) larva
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, put the larva of the chrysomelid worm of horseradish ape (Phaedoncochleariae).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all mealworms of expression all are killed; 0% expression does not have mealworm to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table G
Destroy the insect of plant
The test of daikon leaf beetle (Phaedon) larva
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment H
Knurl volume Aphis (Myzus) test
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling the cabbage leaves (Brassica oleracea) of severe infections black peach aphid (Myzus persicae) in the active agent preparations that immerses desired concn.
Behind required time, measure the kill ratio of representing with %.Wherein 100% all aphids of expression all are killed; 0% expression does not have aphid to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table H
Destroy the insect of plant
The test of knurl volume Aphis
Figure S061A0199020060720D000301
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Example I
Noctuid (Spodoptera frugiperda) test is coveted on the meadow
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, put the caterpillar of mythimna separata (noctuid is coveted on the meadow).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table I
Destroy the insect of plant
The greedy noctuid test in meadow
Figure S061A0199020060720D000311
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment J
Cotton bollworm (Heliothis armigera) test
Solvent: 7 weight portion dimethyl formamides
Emulsifier: the alkylaryl polyglycol ether of 2 weight portions
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Soybean spray (Glycine max) through handling in the active agent preparations that immerses desired concn, and is put cotton bollworm (Heliothis armigera) caterpillar when Soybean Leaves is still moist.
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table J
Destroy the insect of plant
The cotton bollworm test
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment K
The test of daikon leaf beetle (Phaedon) larva
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, put the larva of the chrysomelid worm of horseradish ape (Phaedoncochleariae).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all mealworms of expression all are killed; 0% expression does not have mealworm to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table K
Destroy the insect of plant
The test of daikon leaf beetle (Phaedon) larva
Figure S061A0199020060720D000331
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment L
Plutella (Plutella) test, the responsive system of planting
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, the put diamond-back moth caterpillar of (Plutellaxylostella, the responsive system of planting).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table L
Destroy the insect of plant
The Plutella test, the responsive system of planting
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment M
Plutella (Plutella) test, resistance kind system
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, the put diamond-back moth caterpillar of (Plutellaxylostella, resistance kind system).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table M
Destroy the insect of plant
The Plutella test, resistance kind system
Figure S061A0199020060720D000351
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment N
Noctuid (Spodoptera frugiperda) test is coveted on the meadow
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, put the caterpillar of mythimna separata (noctuid is coveted on the meadow).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table N
Destroy the insect of plant
The greedy noctuid test in meadow
Figure S061A0199020060720D000361
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment O
Cotten aphid (Aphis gossypii) test
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling the cotton leaf (Gossypium hirsutum) of severe infections cotten aphid (Aphis gossypii) in the active agent preparations that immerses desired concn.
Behind required time, measure the kill ratio of representing with %.Wherein 100% all aphids of expression all are killed; 0% expression does not have aphid to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table O
Destroy the insect of plant
The cotten aphid test
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment P
Knurl volume Aphis (Myzus) test
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling the cabbage leaves (Brassica oleracea) of severe infections black peach aphid (Myzus persicae) in the active agent preparations that immerses desired concn.
Behind required time, measure the kill ratio of representing with %.Wherein 100% all aphids of expression all are killed; 0% expression does not have aphid to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table P
Destroy the insect of plant
The test of knurl volume Aphis
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment Q
The test of daikon leaf beetle (Phaedon) larva
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that closes emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, put the larva of the chrysomelid worm of horseradish ape (Phaedoncochleariae).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all mealworms of expression all are killed; 0% expression does not have mealworm to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table Q
Destroy the insect of plant
The test of daikon leaf beetle (Phaedon) larva
Figure S061A0199020060720D000391
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated
Embodiment R
Plutella (Plutella) test, the responsive system of planting
Solvent: 7 weight portion dimethyl formamides
Emulsifier: 2 weight portion alkylaryl polyglycol ethers
For preparing suitable active agent preparations, with the solvent and the emulsifier of 1 weight portion reactive compound and above-mentioned amount, and with the water dilution concentrate that contains emulsifier to desired concn.
Through handling in the active agent preparations that cabbage leaves (Brassica oleracea) is immersed desired concn, and when leaf is still moist, the put diamond-back moth caterpillar of (Plutellaxylostella, the responsive system of planting).
Behind required time, measure the kill ratio of representing with %.Wherein 100% all caterpillars of expression all are killed; 0% expression does not have caterpillar to be killed.Use the kill ratio of being measured in the Carpenter formula, to calculate.
In this test, following reactive compound combination of the present invention is compared with the reactive compound of using separately, has shown the synergistic activity that strengthens.
Table R
Destroy the insect of plant
The Plutella test, the responsive system of planting
Figure S061A0199020060720D000401
The activity of measured value *=practical measurement
Calculated value * *=use Carpenter formula activity calculated

Claims (5)

1. be used to prevent and treat the composition of animal pest, wherein comprise Clothianidin shown in the following formula (I)
Figure FFW00000047333500011
With a kind of synergistic activity mixture that is selected from the compound of β-cyfloxylate or λ-cyhalothrin, wherein the weight ratio of Clothianidin and β-cyfloxylate or λ-cyhalothrin is 1: 1-10: in 1 the scope.
2. the composition that is used to prevent and treat animal pest of claim 1 wherein comprises the synergistic activity mixture of Clothianidin and β-cyfloxylate.
3. the composition that is used to prevent and treat animal pest of claim 1 wherein comprises the synergistic activity mixture of Clothianidin and λ-cyhalothrin.
4. the application of each composition in the control animal pest among the claim 1-3.
5. prepare the method for insecticide, it is characterized in that, each synergistic activity mixture among the claim 1-3 is mixed with incremental agent and/or surfactant.
CN2006101001990A 2002-01-31 2003-01-20 Synergistic insecticidal mixtures Expired - Lifetime CN1895048B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10203688.8 2002-01-31
DE10203688A DE10203688A1 (en) 2002-01-31 2002-01-31 Synergistic insecticidal mixtures

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
CNB038076918A Division CN100360028C (en) 2002-01-31 2003-01-20 Synergistic insecticidal mixtures

Publications (2)

Publication Number Publication Date
CN1895048A CN1895048A (en) 2007-01-17
CN1895048B true CN1895048B (en) 2012-04-11

Family

ID=7713432

Family Applications (3)

Application Number Title Priority Date Filing Date
CNB038076918A Expired - Lifetime CN100360028C (en) 2002-01-31 2003-01-20 Synergistic insecticidal mixtures
CN2007100067463A Expired - Lifetime CN101107929B (en) 2002-01-31 2003-01-20 Synergistic insecticidal mixtures
CN2006101001990A Expired - Lifetime CN1895048B (en) 2002-01-31 2003-01-20 Synergistic insecticidal mixtures

Family Applications Before (2)

Application Number Title Priority Date Filing Date
CNB038076918A Expired - Lifetime CN100360028C (en) 2002-01-31 2003-01-20 Synergistic insecticidal mixtures
CN2007100067463A Expired - Lifetime CN101107929B (en) 2002-01-31 2003-01-20 Synergistic insecticidal mixtures

Country Status (26)

Country Link
US (2) US7097848B2 (en)
EP (2) EP1473997B1 (en)
KR (1) KR100992946B1 (en)
CN (3) CN100360028C (en)
AR (1) AR038323A1 (en)
AT (1) ATE550941T1 (en)
AU (2) AU2003202575B2 (en)
BR (2) BR122013019371B1 (en)
CA (1) CA2474086C (en)
CO (1) CO5600986A2 (en)
DE (1) DE10203688A1 (en)
DK (1) DK1473997T3 (en)
EG (1) EG23409A (en)
ES (2) ES2382535T3 (en)
HR (1) HRP20040789B1 (en)
IL (1) IL163106A (en)
ME (1) MEP11008A (en)
MX (1) MXPA04007298A (en)
NZ (1) NZ534368A (en)
PL (2) PL213691B1 (en)
PT (1) PT1473997E (en)
RS (1) RS52708B (en)
SI (2) SI1473997T1 (en)
UA (1) UA78280C2 (en)
WO (1) WO2003063592A1 (en)
ZA (1) ZA200405968B (en)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6436976B1 (en) 1998-06-10 2002-08-20 Bayer Aktiengesellschaft Agents for combating plant pests
DE10347440A1 (en) * 2003-10-13 2005-05-04 Bayer Cropscience Ag Synergistic insecticidal mixtures
EP1922930A3 (en) * 2004-03-16 2013-02-20 Syngenta Participations AG Pesticidal composition and method for seed treatment
US8133499B2 (en) * 2004-03-25 2012-03-13 Fmc Corporation Liquid termiticide compositions of pyrethroids and neonicitinoids
DE102004032418A1 (en) * 2004-04-07 2005-10-27 Bayer Cropscience Ag Drug combinations with insecticidal properties
DE102004033289A1 (en) * 2004-04-24 2005-11-10 Bayer Cropscience Ag Synergistic insecticidal mixtures
DE102004062512A1 (en) * 2004-12-24 2006-07-06 Bayer Cropscience Ag Synergistic mixtures with insecticidal and fungicidal action
JP2006219463A (en) * 2005-02-14 2006-08-24 Chemiprokasei Kaisha Ltd Wood vermin-controlling composition
EP2269450A3 (en) * 2005-02-24 2011-03-09 Syngenta Participations AG. Method of improving nematode tolerant or resistant plant growth
AR056290A1 (en) * 2005-03-31 2007-10-03 Nippon Soda Co METHOD FOR INHIBITING THE PRODUCTION OF MICOTOXIN
AU2006233601A1 (en) * 2005-04-08 2006-10-19 Syngenta Participations Ag. Method of mollusc control
US20070099963A1 (en) * 2005-11-01 2007-05-03 Bayer Cropscience Lp Nematicidal compositions and methods
DE102006014487A1 (en) * 2006-03-29 2007-10-04 Bayer Cropscience Ag Active agent combination, useful e.g. to combat animal pest and for producing insecticidal and acaricidal agent, comprises a chloropyridine-furanone compound and clothianidin compound
MX2009002433A (en) * 2006-09-12 2009-04-07 Nippon Soda Co Pest control agent in form of stable suspension.
US20120021905A1 (en) * 2009-02-11 2012-01-26 Basf Se Pesticidal Mixtures
WO2010092031A2 (en) * 2009-02-11 2010-08-19 Basf Se Pesticidal mixtures
CN102232385A (en) * 2010-04-25 2011-11-09 青岛凯源祥化工有限公司 Insecticidal composition containing clothianidin and abamectin
JP5712504B2 (en) 2010-04-27 2015-05-07 住友化学株式会社 Pest control composition and use thereof
HUE032446T2 (en) 2010-04-27 2017-09-28 Sumitomo Chemical Co Pesticidal composition and its use
RU2556404C2 (en) 2010-04-28 2015-07-10 Сумитомо Кемикал Компани, Лимитед Pesticidal composition and use thereof
JP5724211B2 (en) 2010-04-28 2015-05-27 住友化学株式会社 Plant disease control composition and use thereof
UA109901C2 (en) 2010-04-28 2015-10-26 COMPOSITION FOR CONTROLLING PLANT DISEASES AND ITS APPLICATION
WO2012124795A1 (en) * 2011-03-17 2012-09-20 Sumitomo Chemical Company, Limited Pest control composition and pest control method
CN102379308A (en) * 2011-09-21 2012-03-21 江苏扬农化工股份有限公司 Mixed insecticidal composition containing clothianidin and application of mixed insecticidal composition
CN102365970A (en) * 2011-09-30 2012-03-07 山东京蓬生物药业股份有限公司 Synergistic pesticidal composition containing Clothianidin and emamectin benzoate, and its application
CN102428951A (en) * 2012-01-14 2012-05-02 陕西美邦农药有限公司 Insecticidal composition containing Clothianidin
JP2015506379A (en) * 2012-02-08 2015-03-02 バイエル・インテレクチユアル・プロパテイー・ゲー・エム・ベー・ハー Active compound composition for vector control of insecticide resistant pests
CN102763672B (en) * 2012-08-13 2014-01-08 广西汇丰生物科技有限公司 Granula containing ivermectin and clothianidin
CN103621537A (en) * 2012-08-29 2014-03-12 南京华洲药业有限公司 Synergistic insecticidal composition containing clothianidin and banleptm and applications thereof
EA030236B1 (en) * 2012-11-30 2018-07-31 Байер Кропсайенс Акциенгезельшафт Ternary fungicidal and pesticidal mixtures
CN103798275A (en) * 2014-02-21 2014-05-21 罗晓丹 Pesticide granules for preventing and curing sugarcane underground pests
CN103875704A (en) * 2014-03-19 2014-06-25 黄业新 Pesticide granules containing clothianidin and diazinon
CN105432666B (en) * 2015-11-19 2018-07-31 广州万粤知识产权运营有限公司 A kind of composition pesticide containing Dipel
CN106386842A (en) * 2016-08-17 2017-02-15 陕西西大华特科技实业有限公司 An insecticidal composition containing clothianidin and lambda-cyhalothrin
CN106508948B (en) * 2016-10-27 2019-03-26 山东润博生物科技有限公司 A kind of suspension seed-coating agent containing avermectin and clothianidin and its application
CN107156168A (en) * 2017-06-21 2017-09-15 天峨县平昌生态农业有限公司 A kind of Pesticidal combination for being used to prevent and treat diamondback moth
CN109907073B (en) * 2018-11-06 2024-02-23 宁夏大学 Biological pesticide for preventing and treating whiteflies and application thereof
CN111011368A (en) * 2019-11-11 2020-04-17 南京华洲药业有限公司 Composite insecticidal and acaricidal nano-water agent containing efficient cyhalothrin and emamectin benzoate and application thereof
CN111084191B (en) * 2019-12-25 2022-02-25 南京保丰农药有限公司 Clothianidin and efficient cyfluthrin suspending agent and preparation method thereof
CN112956480A (en) * 2021-02-04 2021-06-15 四川眉山凯尔化工有限公司 Pesticide raw material formula
CN117598324A (en) * 2023-11-21 2024-02-27 西南大学 Beauveria bassiana-based pesticide for controlling Bactrocera dorsalis and testing method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1149532A1 (en) * 2000-04-26 2001-10-31 Takeda Chemical Industries, Ltd. Method for controlling flies

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3313684A (en) 1959-12-05 1967-04-11 Bayer Ag 3, 5-dimethyl-4-methylmercaptophenyl n-methyl carbamate and methods for combating insects
SE434277B (en) 1976-04-19 1984-07-16 Merck & Co Inc SET TO MAKE NEW ANTIHELMINTICALLY EFFECTIVE ASSOCIATIONS BY CULTIVATING STREPTOMYCS AVERMITILIS
US4427663A (en) 1982-03-16 1984-01-24 Merck & Co., Inc. 4"-Keto-and 4"-amino-4"-deoxy avermectin compounds and substituted amino derivatives thereof
ZA836964B (en) 1982-10-11 1984-05-30 Ici Plc Insecticidal product and preparation thereof
GB8308507D0 (en) 1983-03-28 1983-05-05 Ici Plc Insecticidal product
EP0106469B1 (en) 1982-10-11 1987-01-14 Imperial Chemical Industries Plc Insecticidal product and preparation thereof
DE3522629A1 (en) 1985-06-25 1987-01-08 Bayer Ag METHOD FOR PRODUCING SPECIFIC ENANTIOMER PAIRS OF PERMETHRINIC ACID (ALPHA) CYANO-3-PHENOXY-4-FLUOR-BENZYL ESTERS
US4874749A (en) 1987-07-31 1989-10-17 Merck & Co., Inc. 4"-Deoxy-4-N-methylamino avermectin Bla/Blb
US5238949A (en) 1988-11-29 1993-08-24 Nihon Bayer Agrochem K.K. Insecticidally active nitro pyridyl compounds
JP2779403B2 (en) 1988-11-29 1998-07-23 日本バイエルアグロケム株式会社 Insecticidal nitro compounds
IE960442L (en) 1988-12-27 1990-06-27 Takeda Chemical Industries Ltd Guanidine derivatives, their production and insecticides
ES2059841T3 (en) 1989-02-13 1994-11-16 Bayer Agrochem Kk NITRO COMPOUNDS WITH INSECTICIDE ACTIVITY.
US5204359A (en) 1989-02-13 1993-04-20 Nihon Bayer Agrochem K.K. Insecticidally active nitro compounds
US4874794A (en) 1989-04-28 1989-10-17 Lidak Biopharmaceuticals Inflammatory disease treatment
IL98599A (en) 1990-06-28 1995-06-29 Merck & Co Inc Stable salts of 4"-deoxy-4"-epi-methylamino avermectin b1a/b1b and insecticidal compositions containing them
US6828275B2 (en) * 1998-06-23 2004-12-07 Bayer Aktiengesellschaft Synergistic insecticide mixtures
DE19823396A1 (en) * 1998-05-26 1999-12-02 Bayer Ag Synergistic insecticidal mixtures
UA65624C2 (en) * 1998-07-02 2004-04-15 Елі Ліллі Енд Компані Pediculicidal formulation for hair care (variants) and methods of controlling lice infestation using spinosyn (variants)
RU2001117068A (en) * 1998-11-20 2003-06-27 Байер Акциенгезельшафт (De) COMBINATIONS OF SUBSTANCES WITH FUNGICIDAL ACTIVITY
US6586617B1 (en) * 1999-04-28 2003-07-01 Sumitomo Chemical Takeda Agro Company, Limited Sulfonamide derivatives
US6927210B1 (en) * 1999-08-12 2005-08-09 Eli Lilly And Company Ectoparasiticidal aqueous suspension formulations of spinosyns
MY138097A (en) * 2000-03-22 2009-04-30 Du Pont Insecticidal anthranilamides
US6660690B2 (en) * 2000-10-06 2003-12-09 Monsanto Technology, L.L.C. Seed treatment with combinations of insecticides
US6838473B2 (en) * 2000-10-06 2005-01-04 Monsanto Technology Llc Seed treatment with combinations of pyrethrins/pyrethroids and clothiandin

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1149532A1 (en) * 2000-04-26 2001-10-31 Takeda Chemical Industries, Ltd. Method for controlling flies

Also Published As

Publication number Publication date
ES2382535T3 (en) 2012-06-11
EP2272367B1 (en) 2012-03-28
AU2008243057A1 (en) 2008-11-27
YU66004A (en) 2006-08-17
PL371434A1 (en) 2005-06-13
HRP20040789B1 (en) 2013-07-31
EP1473997B1 (en) 2012-11-28
PL394622A1 (en) 2011-08-16
CN1895048A (en) 2007-01-17
IL163106A (en) 2010-05-31
EP2272367A1 (en) 2011-01-12
WO2003063592A1 (en) 2003-08-07
MXPA04007298A (en) 2004-10-29
AU2008243057B2 (en) 2011-11-24
MEP11008A (en) 2010-06-10
US7097848B2 (en) 2006-08-29
DK1473997T3 (en) 2013-02-04
PL213691B1 (en) 2013-04-30
CN1646017A (en) 2005-07-27
CA2474086C (en) 2012-03-27
ES2400288T3 (en) 2013-04-08
US20060194747A1 (en) 2006-08-31
BR0307356A (en) 2004-12-14
HRP20040789A2 (en) 2005-02-28
BR122013019371B1 (en) 2015-07-14
CO5600986A2 (en) 2006-01-31
ATE550941T1 (en) 2012-04-15
AR038323A1 (en) 2005-01-12
CN101107929A (en) 2008-01-23
SI2272367T1 (en) 2012-07-31
BR0307356B1 (en) 2014-10-07
CA2474086A1 (en) 2003-08-07
ZA200405968B (en) 2005-10-26
AU2003202575B2 (en) 2008-11-13
PT1473997E (en) 2013-01-29
US20050222051A1 (en) 2005-10-06
CN101107929B (en) 2010-06-16
EP1473997A1 (en) 2004-11-10
UA78280C2 (en) 2007-03-15
EG23409A (en) 2005-06-21
PL212915B1 (en) 2012-12-31
NZ534368A (en) 2006-02-24
RS52708B (en) 2013-08-30
CN100360028C (en) 2008-01-09
SI1473997T1 (en) 2013-02-28
KR20040086280A (en) 2004-10-08
KR100992946B1 (en) 2010-11-08
DE10203688A1 (en) 2003-08-07

Similar Documents

Publication Publication Date Title
CN1895048B (en) Synergistic insecticidal mixtures
CN100438764C (en) Synergistic insecticide mixtures
CN100374419C (en) Cis-alkoxy-substituted spirocyclic 1-h-pyrrolidine-2,4-dione derivatives serving as pesticides
JP4755761B2 (en) Synergistic insecticide mixture
TWI228121B (en) Active compound combinations having insecticidal properties
JP4922927B2 (en) Synergistic insecticide mixture
CN100496243C (en) Synergistic insecticidal mixtures
PL209244B1 (en) Fungicidal active substance combinations containing trifloxystrobin
JP2009514908A (en) Synergistic insecticidal mixture for treating seeds
CN1307155C (en) Deltal-pyrrolines used as pesticides
CN100508753C (en) Synergistic insecticidal mixtures
CN1312138C (en) Novel azoles having an insecticidal action
ES2296903T3 (en) SYNERGIC MIXTURES OF PESTICIDES AGAINST ANIMNAL PESTS.
JP2007513108A (en) Synergistic insecticide mixture
CN100448877C (en) 3-phenyl substituted 3-substituted-4ketolactams and ketolactones
CN100415097C (en) Synergistic pesticide mixtures for the control of animal pests
CN100374424C (en) Heterocyclic amide derivative and use as pesticide
CN101128413A (en) Substituted oxyarenes
CN100376566C (en) Delta1-pyrrolines compound
CN1474651A (en) Use of riboflavin and flavin derivatives as chitinase inhibitors

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C12 Rejection of a patent application after its publication
RJ01 Rejection of invention patent application after publication

Open date: 20070117

C14 Grant of patent or utility model
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20170713

Address after: German Monheim

Patentee after: BAYER INTELLECTUAL PROPERTY GmbH

Address before: German Monheim

Patentee before: BAYER CROPSCIENCE AG

TR01 Transfer of patent right
CX01 Expiry of patent term

Granted publication date: 20120411

CX01 Expiry of patent term